Expression of neutral endopeptidase activity during clinical and experimental acute lung injury

<p>Abstract</p> <p>Background</p> <p>Neutral endopeptidase (NEP), an enzyme that cleaves inflammatory bioactive peptides, may play a protective role in the pathogenesis of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). However, its low extracell...

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Main Authors: Kiuchi Kazutoshi, Oh-hashi Kentaro, Amaya Fumimasa, Hashimoto Soshi, Hashimoto Satoru
Format: Article
Language:English
Published: BMC 2010-11-01
Series:Respiratory Research
Online Access:http://respiratory-research.com/content/11/1/164
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spelling doaj-a910dc5baab04d1bb1f69cabe577189a2020-11-24T21:52:51ZengBMCRespiratory Research1465-99212010-11-0111116410.1186/1465-9921-11-164Expression of neutral endopeptidase activity during clinical and experimental acute lung injuryKiuchi KazutoshiOh-hashi KentaroAmaya FumimasaHashimoto SoshiHashimoto Satoru<p>Abstract</p> <p>Background</p> <p>Neutral endopeptidase (NEP), an enzyme that cleaves inflammatory bioactive peptides, may play a protective role in the pathogenesis of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). However, its low extracellular activity hinders the precise measurement of changes that take place during ALI/ARDS. The main objective of this study was to clarify the regulation of NEP activity and its expression during ALI/ARDS.</p> <p>Methods</p> <p>In a <it>clinical study</it>, we measured plasma NEP activity in patients who developed postoperative ALI/ARDS, using a HPLC fluorometric system. In an <it>experimental study</it>, we induced ALI by intratracheal instillation of hydrochloric acid (HCl) or lipopolysaccharide (LPS) in mice, and similarly measured NEP activity in plasma, lung tissue, and broncho-alveolar lavage fluid (BALF). We also studied the distribution and measured the amounts of NEP protein, using immuno-histochemical and immunoblot analyses, and measured the levels of NEP mRNA, using real-time reverse transcription-polymerase chain reaction, in the lungs of mice with ALI.</p> <p>Results</p> <p>The plasma NEP activity was significantly lower in patients presenting with ALI/ARDS than in controls. Similarly, the NEP activity in plasma and lung tissue was markedly lower, and lung injuries more severe in LPS- than in HCl-treated mice. In contrast, the activity of NEP in the BALF of LPS-treated mice was increased. The intratracheal instillation of LPS decreased the gene expression of NEP in the lung. Immuno-histochemical and Western immunoblot studies in mice confirmed a) the presence of NEP in the alveolar wall, a critical target in ALI/ARDS, and b) a decrease in its expression in HCl- and LPS-induced ALI.</p> <p>Conclusion</p> <p>In this experimental and clinical study of ALI/ARDS, the activity of NEP was significantly decreased in plasma and increased in the alveolar air space.</p> http://respiratory-research.com/content/11/1/164
collection DOAJ
language English
format Article
sources DOAJ
author Kiuchi Kazutoshi
Oh-hashi Kentaro
Amaya Fumimasa
Hashimoto Soshi
Hashimoto Satoru
spellingShingle Kiuchi Kazutoshi
Oh-hashi Kentaro
Amaya Fumimasa
Hashimoto Soshi
Hashimoto Satoru
Expression of neutral endopeptidase activity during clinical and experimental acute lung injury
Respiratory Research
author_facet Kiuchi Kazutoshi
Oh-hashi Kentaro
Amaya Fumimasa
Hashimoto Soshi
Hashimoto Satoru
author_sort Kiuchi Kazutoshi
title Expression of neutral endopeptidase activity during clinical and experimental acute lung injury
title_short Expression of neutral endopeptidase activity during clinical and experimental acute lung injury
title_full Expression of neutral endopeptidase activity during clinical and experimental acute lung injury
title_fullStr Expression of neutral endopeptidase activity during clinical and experimental acute lung injury
title_full_unstemmed Expression of neutral endopeptidase activity during clinical and experimental acute lung injury
title_sort expression of neutral endopeptidase activity during clinical and experimental acute lung injury
publisher BMC
series Respiratory Research
issn 1465-9921
publishDate 2010-11-01
description <p>Abstract</p> <p>Background</p> <p>Neutral endopeptidase (NEP), an enzyme that cleaves inflammatory bioactive peptides, may play a protective role in the pathogenesis of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). However, its low extracellular activity hinders the precise measurement of changes that take place during ALI/ARDS. The main objective of this study was to clarify the regulation of NEP activity and its expression during ALI/ARDS.</p> <p>Methods</p> <p>In a <it>clinical study</it>, we measured plasma NEP activity in patients who developed postoperative ALI/ARDS, using a HPLC fluorometric system. In an <it>experimental study</it>, we induced ALI by intratracheal instillation of hydrochloric acid (HCl) or lipopolysaccharide (LPS) in mice, and similarly measured NEP activity in plasma, lung tissue, and broncho-alveolar lavage fluid (BALF). We also studied the distribution and measured the amounts of NEP protein, using immuno-histochemical and immunoblot analyses, and measured the levels of NEP mRNA, using real-time reverse transcription-polymerase chain reaction, in the lungs of mice with ALI.</p> <p>Results</p> <p>The plasma NEP activity was significantly lower in patients presenting with ALI/ARDS than in controls. Similarly, the NEP activity in plasma and lung tissue was markedly lower, and lung injuries more severe in LPS- than in HCl-treated mice. In contrast, the activity of NEP in the BALF of LPS-treated mice was increased. The intratracheal instillation of LPS decreased the gene expression of NEP in the lung. Immuno-histochemical and Western immunoblot studies in mice confirmed a) the presence of NEP in the alveolar wall, a critical target in ALI/ARDS, and b) a decrease in its expression in HCl- and LPS-induced ALI.</p> <p>Conclusion</p> <p>In this experimental and clinical study of ALI/ARDS, the activity of NEP was significantly decreased in plasma and increased in the alveolar air space.</p>
url http://respiratory-research.com/content/11/1/164
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